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Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Clinical Genetics|September 24, 2017
Detection of copy number variations in epilepsy using exome dataN Tsuchida, M Nakashima, M Kato, et al.
Clinical Genetics|July 20, 2016
Molecular genetic analysis of 30 families with Joubert syndromeT Suzuki, N Miyake, Y Tsurusaki, et al.
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